Peer-reviewed veterinary case report
Efficacy of LASER for de-epithelialization of free gingival graft: a systematic review.
- Year:
- 2025
- Authors:
- Hazrati P et al.
- Affiliation:
- University of Michigan-Ann Arbor · United States
Abstract
This systematic review primarily aimed to investigate the efficacy of de-epithelializing free gingival graft (FGG) using LASER and, secondarily, to evaluate the clinical outcomes of soft tissue augmentation using LASER-de-epithelialized connective tissue grafts (CTGs). Following PRISMA guidelines, an electronic search was conducted in PubMed/MEDLINE, Scopus, Embase, and Web of Science databases without date or language restrictions on February 4, 2025. Clinical studies employing LASER for de-epithelializing FGG were considered eligible. The primary outcome was successful epithelium removal, while the main secondary outcomes were mean and complete root coverage percentage. Quality appraisal of the included studies was executed according to the revised Cochrane risk-of-bias tool for randomized trials (RoB2) and Risk of Bias in Non-randomized Studies - of Interventions (ROBINS-I). Of 243 studies, three met all eligibility criteria. Two randomized controlled clinical trials (RCTs), and one pre-post study were included. CO<sub>2</sub>, Er: YAG, and diode LASERs were utilized in the included studies. Power was set to 1 and 2 W in two and one studies, respectively. Epithelium removal was not quantitatively reported in any of the included studies, but complete removal of epithelium with LASER was reported qualitatively in one study. In all the included studies, LASERs yielded clinical outcomes comparable to blades, with minor superiorities in aesthetic outcomes observed with LASERs. LASERs show potential for successful removal of epithelium from FGG without causing safety issues or complications. However, the evidence on this topic remains limited, highlighting the need for well-conducted and reported RCTs. Registration The protocol of this systematic review was registered on PROSPERO with the ID CRD42025646636. Clinical Trial Number Not applicable.
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Search related cases →Original publication: https://europepmc.org/article/MED/40576836